XXY Talk: Greg Brimhall Age 35

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  • เผยแพร่เมื่อ 21 ก.ย. 2024
  • When Greg was diagnosed with Klinefelter syndrome at 15 his parents told him to not tell anyone. Greg knew with time he wouldn’t let his own parents stop him from being himself and being proud of who he was. At 21 he fully accepted himself and has been fully open about teaching people what it like to have Klinefelter syndrome. Www.livingwithxxy.org

ความคิดเห็น • 37

  • @karenjohnson3414
    @karenjohnson3414 4 หลายเดือนก่อน +2

    I like the message of being yourself. Don’t feel that you have to live up to society’s standards. Instead be kind to yourself and accept yourself for who you are. The person God meant you to be all along.

  • @danadams1427
    @danadams1427 11 หลายเดือนก่อน +2

    I really appreciate your courage and activism.

  • @bobweiss7884
    @bobweiss7884 3 ปีที่แล้ว +2

    I've had 47xxy. I'm a 56yr old man I found out when I was 16. I have lots of health issues. Now the biggest is my Heart. So some of us aren't as lucky as others.

  • @rebeccadejong5087
    @rebeccadejong5087 4 ปีที่แล้ว +6

    Great video, thanks for sharing!

  • @matthewtatham5461
    @matthewtatham5461 4 ปีที่แล้ว +4

    So amazing!!!!

  • @freerider604
    @freerider604 4 ปีที่แล้ว +6

    Through investigation of my own I connected with doctors and specialists which led to my diagnoses at 21. My parents had no idea why I had learning disabilities - I guess they just thought I was slow. During my 20’s living with Kleinfelters; my Endocronoligist at the time said that Testerone supplements weren’t necessary 😭. I didn’t start taking Testerone shots until I was in my 30’s. I’m 45 now, still shy, still have learning disabilities, I never felt connected to any kind of group, I prefer being alone (although I am married w/ 3 step-kids), never had any confidence or coordination to play sports. 😂😳

    • @ponchobrimhall
      @ponchobrimhall 4 ปีที่แล้ว +1

      I never really played sports until I found skiing and mountain biking. But I also love building things and video games

    • @freerider604
      @freerider604 4 ปีที่แล้ว +1

      greg brimhall ya I love mountain biking too! And ya video games - my building skills aren’t the greatest but I’m gonna start building model cars 😂

    • @peterrodby2786
      @peterrodby2786 2 ปีที่แล้ว

      @Peter McMullin I found this comment section only by clicking on Klinefelters. I was diagnosed with KS in 1995 when I was 30 y/o. Tomorrow I'll be getting a testopel implant meaning no more shots, gel or patches. My wife of twenty years loves me unconditionally however I have always been into fitness once I escaped from morbid obesity in my youth. I hope this next phase can help me lose that visceral fat I've been fighting to lose since the mid 1980's. I hope all is well with you.

  • @user-vi2dk1qz5f
    @user-vi2dk1qz5f ปีที่แล้ว

    Great channel. Happy these folks have it.

  • @mnfourmn
    @mnfourmn 4 ปีที่แล้ว +3

    Thank you for sharing

  • @jay3974
    @jay3974 4 ปีที่แล้ว +5

    Awesome! Thanks for sharing. My fiance has xxy

    • @LivingwithXXY
      @LivingwithXXY  3 ปีที่แล้ว

      Thanks for watching!

    • @adityaRaj-uh7es
      @adityaRaj-uh7es 3 ปีที่แล้ว +1

      Its good to see that you are still with him, even after knowing this. Are you concerned about not being able to have kids?

  • @VrickzGamer
    @VrickzGamer 3 ปีที่แล้ว +2

    I am very depressed with this disease

  • @johnnyb793
    @johnnyb793 4 ปีที่แล้ว +3

    Can u make a vid explaining why u taken a lot of MRI’s over the years
    My mri test said I had a pituitary microadenoma which my doc said don’t worry looks normal but to go take another one on December

  • @yousufrazavlogs
    @yousufrazavlogs 3 ปีที่แล้ว +1

    Sir me too XXY person should I go for surgery for baby tesa or IVF

  • @anindianhomosapien7189
    @anindianhomosapien7189 4 ปีที่แล้ว +1

    😇

  • @WDBsirLocksight
    @WDBsirLocksight 3 ปีที่แล้ว

    I've been trying to get multidisciplinary care for my complex case with KS.
    Where's the defrag for the medical system...?

    • @LivingwithXXY
      @LivingwithXXY  3 ปีที่แล้ว

      No one with xxy talks about it so no one knows it even exists.

  • @Kremlinbot-mz1cm
    @Kremlinbot-mz1cm 4 ปีที่แล้ว +1

    Hi, i have one question. Does your hands and legs is cold?

  • @truth28
    @truth28 4 ปีที่แล้ว

    Hi, how long did it take for the auto injector to arrive after ordering?

    • @LivingwithXXY
      @LivingwithXXY  4 ปีที่แล้ว

      Ant a few days. It comes from Europe

    • @truth28
      @truth28 4 ปีที่แล้ว

      Living with XXY thank you my brotha!

  • @wabbadu1
    @wabbadu1 4 ปีที่แล้ว

    is getting tested for Klinefelter's Syndrome covered by health insurance?

    • @LivingwithXXY
      @LivingwithXXY  3 ปีที่แล้ว +1

      Depending on what insurance you have.

  • @ricardopadilla7859
    @ricardopadilla7859 4 ปีที่แล้ว

    *I have a question for you.*
    *Have you had nocturnal emission?*

    • @LivingwithXXY
      @LivingwithXXY  4 ปีที่แล้ว +1

      Santino Palacios Maybe once when I was 13 but I can’t remember. Why?

    • @ricardopadilla7859
      @ricardopadilla7859 4 ปีที่แล้ว

      @@LivingwithXXY because I've heard that people with klinefelter syndrom almost don't have emission nocturnal.
      But in your case seem you can reproduce 👍.

    • @LivingwithXXY
      @LivingwithXXY  4 ปีที่แล้ว +1

      Don’t believe everything you read on the internet about Klinefelter syndrome. It’s a spectrum.

    • @ricardopadilla7859
      @ricardopadilla7859 4 ปีที่แล้ว

      @@LivingwithXXY ok my friend , sorry for information little sure , I also asked this man with your same syndrom
      th-cam.com/video/tKQofPU-wX4/w-d-xo.html
      He have never heard about emission nocturnal and for that I had many dudes with your case but the important is good to know, regard from Ecuador 🇪🇨 🖐😊

    • @NinoskaMariaPaz
      @NinoskaMariaPaz 3 ปีที่แล้ว

      Thanks